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Spanlastics gel-A novel drug carrier for transdermal delivery of glimepiride.
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- Journal of Liposome Research, 2023, v. 33, n. 1, p. 102, doi. 10.1080/08982104.2022.2100902
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- Publication type:
- Article
Haemolytic anaemia and hepatocitolysis associated with hypermagnesaemia by repeated exposures to copper-calcium fungicides.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2018, v. 33, n. 1, p. 184, doi. 10.1080/14756366.2017.1409745
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- Publication type:
- Article
Heterozygous SOD1 deficiency in mice with an NZW background causes male infertility and an aberrant immune phenotype.
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- Free Radical Research, 2019, v. 53, n. 11/12, p. 1060, doi. 10.1080/10715762.2019.1677901
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- Article
Catastrophic relapse of Evans syndrome five years after allogeneic BMT notwithstanding full donor chimerism. Terminal hemolytic-uremic syndrome
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- Autoimmunity, 2006, v. 39, n. 6, p. 505, doi. 10.1080/08916930600847598
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- Article
Mechanisms of Immunological Tolerance Loss Versus Erythrocyte Self-antigens and Autoimmune Hemolytic Anemia.
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- Autoimmunity, 2003, v. 36, n. 4, p. 199, doi. 10.1080/0891693031000151238
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- Article
Hemolytic-uremic syndrome: Findings of post-acute renal failure in light and electron microscopy.
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- Ultrastructural Pathology, 2017, v. 41, n. 3, p. 227, doi. 10.1080/01913123.2017.1292436
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- Article
Distinct lipid profile in haemolytic anaemia-related gallstones compared with the general gallstone.
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- Annals of Medicine, 2023, v. 55, n. 1, p. 1, doi. 10.1080/07853890.2023.2203514
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- Article
Hemolytic Anemia and Metabolic Acidosis: Think about Glutathione Synthetase Deficiency.
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- Fetal & Pediatric Pathology, 2015, v. 34, n. 1, p. 18, doi. 10.3109/15513815.2014.947543
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- Publication type:
- Article
A Novel and a Previously Described Compound Heterozygous PKLR Gene Mutations Causing Pyruvate Kinase Deficiency in a Chinese Child.
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- Fetal & Pediatric Pathology, 2014, v. 33, n. 3, p. 182, doi. 10.3109/15513815.2014.890260
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- Publication type:
- Article
Catalase deficiency may complicate urate oxidase (rasburicase) therapy.
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- Free Radical Research, 2007, v. 41, n. 9, p. 953, doi. 10.1080/10715760701482451
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- Publication type:
- Article
Kawasaki disease and acute haemolytic anaemia after two IVIG infusions.
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- Biotechnology & Biotechnological Equipment, 2016, v. 30, n. 3, p. 448, doi. 10.1080/13102818.2016.1159529
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- Publication type:
- Article
In vivo activity and atom pair fingerprint analysis of MMV665941 against the apicomplexan parasite Babesia microti, the causative agent of babesiosis in humans and rodents.
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- Pathogens & Global Health, 2023, v. 117, n. 3, p. 315, doi. 10.1080/20477724.2022.2128571
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- Publication type:
- Article
Immune thrombocytopenic purpura in ulcerative colitis: a case report and systematic review.
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- 2014
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- Publication type:
- Case Study
Delayed Onset of Autoimmune Hemolytic Anemia Complicating Cladribine Therapy for Waldenstrom Macroglobulinemia.
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- Leukemia & Lymphoma, 2000, v. 37, n. 1/2, p. 125, doi. 10.3109/10428190009057635
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- Publication type:
- Article
Primary Sclerosing Cholangitis with Autoimmune Hemolytic Anemia and Pulmonary Infiltrations.
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- Scandinavian Journal of Gastroenterology, 1998, v. 33, n. 6, p. 669, doi. 10.1080/00365529850171972
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- Publication type:
- Article
Human genetic variation: New challenges and opportunities for doping control.
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- Journal of Sports Sciences, 2012, v. 30, n. 11, p. 1117, doi. 10.1080/02640414.2012.692480
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- Publication type:
- Article
Glutathione synthetase deficiency: a novel mutation with femur agenesis.
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- Fetal & Pediatric Pathology, 2020, v. 39, n. 1, p. 38, doi. 10.1080/15513815.2019.1627627
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- Publication type:
- Article
Tokyo-1 Mutation: Hereditary Spherocytosis in a Hispanic Newborn Presenting as Early Onset Severe Hyperbilirubinemia.
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- Fetal & Pediatric Pathology, 2018, v. 37, n. 4, p. 296, doi. 10.1080/15513815.2018.1485797
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- Publication type:
- Article
Diffuse Chorangiomatosis as a Cause of Cardiomegaly, Microangiopathic Hemolytic Anemia and Thrombocytopenia in a Newborn.
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- 2017
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- Publication type:
- Case Study
Intracranial extramedullary haematopoiesis: A case report.
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- 2015
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- Publication type:
- Case Study
Congenital Nonspherocytic Hemolytic Anemia Caused by Krüppel-Like Factor 1 Gene Variants: Another Case Report.
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- Hemoglobin, 2019, v. 43, n. 4/5, p. 292, doi. 10.1080/03630269.2019.1680384
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- Publication type:
- Article
Hb Aalesund (HBA2: c.400_406delAGCACCG), an Unstable α-Globin Variant Found in a Norwegian Patient Causing Moderate Hemolytic Anemia and Falsely High Hb A<sub>1c</sub> Using Ion Exchange High Performance Liquid Chromatography.
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- Hemoglobin, 2019, v. 43, n. 2, p. 122, doi. 10.1080/03630269.2019.1614048
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- Publication type:
- Article
A Homozygous Mutation on the HBA1 Gene Coding for Hb Charlieu (HBA1: c.320T>C) Together with β-Thalassemia Trait Results in Severe Hemolytic Anemia.
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- Hemoglobin, 2019, v. 43, n. 2, p. 77, doi. 10.1080/03630269.2019.1601107
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- Publication type:
- Article
Severe Thalassemia Caused by Hb Zunyi [β147(HC3)Stop→Gln; HBB: c.442T>C)] on the β-Globin Gene.
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- Hemoglobin, 2019, v. 43, n. 1, p. 7, doi. 10.1080/03630269.2019.1582430
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- Publication type:
- Article
Unstable Hemoglobin Variants: The Need for Clinical Vigilance in Infants with Congenital Jaundice.
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- Hemoglobin, 2019, v. 43, n. 1, p. 60, doi. 10.1080/03630269.2019.1582429
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- Publication type:
- Article
Hb Milano [α109(G16)Leu→Pro (CTG>CCG); HBA1: c.329T>C]: A Novel Variant on the α1-Globin Gene in an Italian Family.
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- Hemoglobin, 2019, v. 43, n. 1, p. 4, doi. 10.1080/03630269.2019.1566138
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- Article
Prevalence of α-Thalassemia in the Egyptian Population.
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- Hemoglobin, 2018, v. 42, n. 4, p. 243, doi. 10.1080/03630269.2018.1527231
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- Publication type:
- Article
Clinical Genotyping by Next Generation Sequencing Reveals a Novel, De Novo β-Globin Gene Mutation Causing Hemolytic Anemia in a Chinese Individual.
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- Hemoglobin, 2018, v. 42, n. 3, p. 184, doi. 10.1080/03630269.2018.1496928
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- Publication type:
- Article
Hb Oslo [β42(CD1)Phe→Ile; HBB: c.127T>A]: A Novel Unstable Hemoglobin Variant Found in a Norwegian Patient.
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- Hemoglobin, 2018, v. 42, n. 2, p. 78, doi. 10.1080/03630269.2018.1468773
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- Publication type:
- Article
A Coincidental Discovery of a New Stable Variant (Hb Hachioji or <italic>HBB</italic>: c.187C>T) in a Patient with Chronic Hemolytic Anemia of Unexplained Origin.
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- Hemoglobin, 2018, v. 42, n. 1, p. 1, doi. 10.1080/03630269.2018.1429279
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- Publication type:
- Article
Hb Moscva [β24(B6)Gly→Asp (G<italic>G</italic>T>G<italic>A</italic>T), <italic>HBB</italic>: c.74G>A]: An Unstable Hemoglobin Newly Detected as a <italic>De Novo</italic> Mutation in a Mauritanian Patient.
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- Hemoglobin, 2018, v. 42, n. 1, p. 7, doi. 10.1080/03630269.2018.1428620
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- Article
α -Thalassemia Caused by an 811 bp Deletion in Individuals from Nanning, Guangxi: A Report of Two Cases.
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- 2017
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- Publication type:
- Case Study
α -Thalassemia Due to a 90.7 kb Deletion (– – ).
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- Hemoglobin, 2017, v. 41, n. 3, p. 218, doi. 10.1080/03630269.2017.1369987
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- Article
Prevalence, Incidence, Trend, and Complications of Thalassemia in Iraq.
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- Hemoglobin, 2017, v. 41, n. 3, p. 164, doi. 10.1080/03630269.2017.1354877
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- Publication type:
- Article
Comparison of Quality of Life in Patients with β-Thalassemia Intermedia and β-Thalassemia Major in Southern Iran.
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- Hemoglobin, 2017, v. 41, n. 3, p. 169, doi. 10.1080/03630269.2017.1340307
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- Publication type:
- Article
Hematological and Molecular Characterization of a Novel Hb A 2 Variant with Homozygous α-Thalassemia-2 in a Southern Thai Individual.
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- Hemoglobin, 2017, v. 41, n. 3, p. 213, doi. 10.1080/03630269.2017.1345760
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- Article
First Report of a Novel Deletion Due to εγδβ -Thalassemia in a Chinese Family.
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- Hemoglobin, 2017, v. 41, n. 3, p. 175, doi. 10.1080/03630269.2017.1366918
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- Publication type:
- Article
Prevalence of Thalassemia Traits and Iron Deficiency Anemia in Sindh, Pakistan.
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- Hemoglobin, 2017, v. 41, n. 3, p. 157, doi. 10.1080/03630269.2017.1345759
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- Publication type:
- Article
A Novel 31.1 kb α-Thalassemia Deletion (– – ) Found in a Mexican Family.
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- Hemoglobin, 2017, v. 41, n. 3, p. 180, doi. 10.1080/03630269.2017.1356330
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- Publication type:
- Article
A Multi-locus Approach to Characterization of Major Quantitative Trait Loci Influencing Hb F Regulation in Chinese β-thalassemia Carriers.
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- Hemoglobin, 2016, v. 40, n. 6, p. 400, doi. 10.1080/03630269.2016.1245198
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- Publication type:
- Article
Hb Southampton [ β 106(G8)Leu→Pro; HBB : c.320T>C] and Codons 41/42 (–TTCT; HBB : c.124_127delTTCT) in a Chinese Girl.
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- Hemoglobin, 2017, v. 41, n. 2, p. 134, doi. 10.1080/03630269.2017.1321015
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- Publication type:
- Article
A Novel Mutation of the α2-Globin Gene Causing α -Thalassemia: Hb Nanning ( HBA2 : c.369_370delinsGA).
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- Hemoglobin, 2017, v. 41, n. 1, p. 56, doi. 10.1080/03630269.2017.1302950
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- Publication type:
- Article
Combination of Hb Heze [ β 144(HC1)Lys→Arg; HBB : c.434A>G] and β -Thalassemia in a Chinese Patient with β -Thalassemia Intermedia.
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- Hemoglobin, 2017, v. 41, n. 1, p. 47, doi. 10.1080/03630269.2017.1290652
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- Publication type:
- Article
Mutational Profile of Homozygous β -Thalassemia in Rio de Janeiro, Brazil.
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- Hemoglobin, 2017, v. 41, n. 1, p. 12, doi. 10.1080/03630269.2017.1289958
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- Publication type:
- Article
The Molecular Spectrum of β- and α-Thalassemia Mutations in Non-Endemic Umbria, Central Italy.
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- Hemoglobin, 2016, v. 40, n. 6, p. 371, doi. 10.1080/03630269.2017.1289101
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- Publication type:
- Article
A Case of Fatal Agranulocytosis That Developed in a Patient with β-Thalassemia Major Treated with Deferiprone.
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- Hemoglobin, 2016, v. 40, n. 6, p. 435, doi. 10.1080/03630269.2016.1276929
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- Publication type:
- Article
A comprehensive screening program for β-thalassemia and other hemoglobinopathies in the Hooghly District of West Bengal, India, dealing with 21 137 cases.
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- Hemoglobin, 2016, v. 40, n. 6, p. 396, doi. 10.1080/03630269.2016.1259169
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- Publication type:
- Article
β -Thalassemia gene mutations in Antalya, Turkey: results from a single centre study.
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- Hemoglobin, 2016, v. 40, n. 6, p. 392, doi. 10.1080/03630269.2016.1256818
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- Publication type:
- Article
Genetic Variants at BCL11A and HBS1L-MYB loci Influence Hb F Levels in Chinese Zhuang β -Thalassemia Intermedia Patients.
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- Hemoglobin, 2016, v. 40, n. 6, p. 405, doi. 10.1080/03630269.2016.1253586
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- Publication type:
- Article
First description of the rs45496295 polymorphism of the C/EBPE gene in β-thalassemia intermedia patients.
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- Hemoglobin, 2016, v. 40, n. 6, p. 411, doi. 10.1080/03630269.2016.1252386
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- Publication type:
- Article